Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Schizophrenia and CACNB2[original query] |
---|
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
Lancet (London, England) 2013 Apr 381 (9875): 1371-9. Authors are not available |
Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia. PLoS genetics 2014 Jun 10 (6): e1004345. Juraeva Dilafruz, Haenisch Britta, Zapatka Marc, Frank Josef, , , Witt Stephanie H, Mühleisen Thomas W, Treutlein Jens, Strohmaier Jana, Meier Sandra, Degenhardt Franziska, Giegling Ina, Ripke Stephan, Leber Markus, Lange Christoph, Schulze Thomas G, Mössner Rainald, Nenadic Igor, Sauer Heinrich, Rujescu Dan, Maier Wolfgang, Børglum Anders, Ophoff Roel, Cichon Sven, Nöthen Markus M, Rietschel Marcella, Mattheisen Manuel, Brors Benedi |
Genetic findings are challenging the symptom-based diagnostic classification system of mental disorders. Shanghai archives of psychiatry 2016 Feb 28 (1): 42-7. Zhang Ch |
Risk-Conferring Glutamatergic Genes and Brain Glutamate Plus Glutamine in Schizophrenia. Frontiers in psychiatry 2017 8 79. Bustillo Juan R, Patel Veena, Jones Thomas, Jung Rex, Payaknait Nattida, Qualls Clifford, Canive Jose M, Liu Jingyu, Perrone-Bizzozero Nora Irma, Calhoun Vince D, Turner Jessica A, Gasparovic Charl |
Voltage-gated calcium channel activity and complex related genes and schizophrenia: A systematic investigation based on Han Chinese population. Journal of psychiatric research 2018 10 106 99-105. Zhang Tianxiao, Zhu Li, Ni Tong, Liu Dan, Chen Gang, Yan Zhilan, Lin Huali, Guan Fanglin, Rice John |
Further evidence for the genetic association between CACNA1I and schizophrenia. Hereditas 2018 155 16. Xie Yijun, Huang Di, Wei Li, Luo Xiong-Ji |
Genetic variants associated with psychotic symptoms across psychiatric disorders. Neuroscience letters 2020 Jan 134754. Calabrò Marco, Porcelli Stefano, Crisafulli Concetta, Albani Diego, Kasper Siegfried, Zohar Joseph, Souery Daniel, Montgomery Stuart, Mantovani Vilma, Mendlewicz Julien, Bonassi Stefano, Vieta Eduard, Frustaci Alessandra, Ducci Giuseppe, Landi Stefano, Boccia Stefania, Bellomo Antonello, Di Nicola Marco, Janiri Luigi, Colombo Roberto, Benedetti Francesco, Mandelli Laura, Fabbri Chiara, Serretti Alessand |
AS3MT Polymorphism: A Risk Factor for Epilepsy Susceptibility and Adverse Drug Reactions to Valproic Acid and Oxcarbazepine Treatment in Children From South China. Frontiers in neuroscience 2021 12 15 705297. Fan Xiaomei, Chen Yuna, Lu Jieluan, Li Wenzhou, Li Xi, Guo Huijuan, Chen Qing, Yang Yanxia, Xia Hanbi |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: